Mitochondrial disease


Mitochondria are energy producing machines that are found in all human cells. Mitochondria contain a small set of genes that must work properly to make the energy our bodies require for health. Defects in mitochondrial function caused by mutations in genes that make mitochondria cause debilitating diseases for which there are no cures and treatments are difficult and limited. Some of these diseases are very difficult to diagnose and provide any treatment besides palliative care.

Mitochondrial diseases affect children as well as adults and they are diseases that affect three or more organ systems and lead progressive deterioration. Often mitochondrial diseases can cause isolated symptoms that may include unexplained seizures, low blood counts, abnormal muscle tone or spasms, blindness, deafness, dementia, ataxia (stumbling or tremors), heart failure, or progressive muscle weakness. Very often several organ systems can be affected in sequence, one affecting another and causing them to further deteriorate.

There are over 50 inherited diseases that involve mitochondrial dysfunction.  It is found that more than 1 in 4,000 children born each year will develop a mitochondrial disease by the age of 10. Mitochondrial diseases are devastating just like childhood cancer and both have a range in mortality from 10 to 50% per year, depending on the specific disease. The mitochondrial disease Leigh's syndrome is one of the more lethal mitochondrial diseases with a mortality of about 50% per year after diagnosis.

Recent researchhas shown that mitochondrial DNA mutations are present in one in 250 people with at least one in 5,000 suffering severe disease. This means that out of 2,000 patients who are seen at a general practice, approximately 10 patients have a mutation that has the potential to cause mitochondrial disease or a disease that can involve mitochondrial dysfunction. 

Mitochondrial medicine research at the Perkins
The Mitochondrial Medicine and Biology Laboratory, headed by Professor Aleksandra Filipovska, investigates the molecular mechanisms that cause mitochondrial diseases. Her team uses cutting edge technologies to identify mutations that cause mitochondrial disease in patients. She investigates how these mutations lead to these disorders to gain insight into potential drug targets. Professor Filipovska’s group is particularly interested in the development of future treatments for mitochondrial diseases.

Back To Top